89941-77-5

Basic information

• Product Name: Methyl 2-methoxytetrahydro-3-furoate
• Synonyms: Methyl 2-methoxytetrahydro-3-furoate;3-Furancarboxylicacid,tetrahydro-2-methoxy-,methylester(9CI);Alkyl-2-alkoxytetrahydro-3-furoate
• CAS NO: 89941-77-5
• Molecular Formula: C₇H₁₂O₄
• Molecular Weight: 160.16778
• Product Categories: CARBOXYLICESTER
• Mol File: 89941-77-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Methyl 2-methoxytetrahydro-3-furoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 2-methoxytetrahydro-3-furoate(89941-77-5)
• EPA Substance Registry System: Methyl 2-methoxytetrahydro-3-furoate(89941-77-5)

Safety Data

• Hazardous Substances Data: 89941-77-5(Hazardous Substances Data)

Usage

Description

Methyl 2-methoxytetrahydro-3-furoate is a synthetic ester with the molecular formula C7H12O4. It is known for its sweet, fruity odor and is commonly used as a flavoring agent and fragrance ingredient in various consumer products.

Uses

Used in Perfume Industry:
Methyl 2-methoxytetrahydro-3-furoate is used as a fragrance ingredient for its sweet, fruity odor, contributing to the overall scent profile of perfumes.
Used in Cosmetics Industry:
Methyl 2-methoxytetrahydro-3-furoate is used as a flavoring agent and fragrance ingredient in cosmetics, enhancing the sensory experience of products such as soaps and lotions.
Used in Food Industry:
Methyl 2-methoxytetrahydro-3-furoate is used as a flavor enhancer in the food industry, particularly for beverages and confectionery items, to improve taste and aroma.
Used in Manufacturing of Scented and Flavored Goods:
Methyl 2-methoxytetrahydro-3-furoate is used as a versatile ingredient in the production of scented and flavored goods due to its stability, solubility, and low volatility.

Upstream product

• 67-56-1 methanol 
• 61541-20-6 methyl 4-hydroxy-2-methylenebutanoate 
• 127915-15-5 2-oxotetrahydrofuran-3-carboxylic acid methyl ester 
• 7647-01-0 hydrogenchloride 
• 53855-26-8 2-formyl-γ-butyrolactone 
• 83124-80-5 3-trichloroacetyl-4,5-dihydrofuran 
• 96-48-0 4-butanolide 
• 107-31-3 Methyl formate 
• 109-94-4 formic acid ethyl ester 

Downstream Products

• 206860-63-1 C₁₇H₂₇Cl₂N₂O₄P 
• 98021-62-6 4,5-dihydrofuran-3-carboxylic acid 
• 65038-86-0 4,5-dihydro-furan-3-carboxylic acid p-toluidide 
• 933770-71-9 α-benzyloxymethyl-γ-lactone 
• 1708-33-4 4-hydroxy-butyraldehyde-(2,4-dinitro-phenylhydrazone) 
• 25714-71-0 4-hydroxybutyraldehyde 
• 53750-81-5 4,5-dihydro-furan-3-carboxylic acid methyl ester 

Relevant articles and documents

HETEROCYCLIC AMIDES AS ROCK INHIBITORS

The present invention relates to new kinase inhibitors of formula (I), more specifically ROCK inhibitors, compositions, in particular pharmaceuticals, comprising such inhibitors, and to uses of such inhibitors in the treatment and prophylaxis of disease. In particular, the present invention relates to new ROCK inhibitors, compositions, in particular pharmaceuticals, comprising such inhibitors, and to uses of such inhibitors in the treatment and prophylaxis of disease. In addition, the invention relates to methods of treatment and use of said compounds in the manufacture of a medicament for the application to a number of therapeutic indications including sexual dysfunction, inflammatory diseases, ophthalmic diseases and Respiratory diseases.

Haloacetylated Enol Ethers: 4. Synthesis of 4-Trihalomethyl-2-methylthiopyrimidines

The synthesis of a series of 5- and 6-substituted 4-trihalomethyl-2-methylthiopyrimidines, prepared from the cyclocondensation reaction of β-alkoxyvinyl trichloromethyl ketones with 2-methyl-2-thiopseudourea sulfate, are reported.A systematic study to find the best reation conditions werre carried out.

STEREOSELECTIVE SYNTHESES OF 2-SUBSTITUTED PERHYDROFUROFURANS

New reagents for the stereoselective synthesis of 2-substituted perhydrofurofurans are described.In the successful approach towards the latter compounds, the key steps were the addition of a monolithio-2α-methoxy-3β-perhydrofuran to an aldehyde and a dilithio-2α-methoxy-3β-perhydrofuran to a carboxyl derivative, respectively.The structures and conformations of the 2-tert-butyl- and 2-isopropylperhydrofurofurans were examined by means of (1)H-NMR double resonance and the 2D-NOE spectroscopy.